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N,N-Diethylaniline → 8-Allyl-7-hydroxy-4-methyl-chromen-2-one

HRID 848153
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HRID 848153 반응식
C([O:4][C:5]1[CH:14]=[C:13]2[C:8]([C:9]([CH3:16])=[CH:10][C:11](=[O:15])[O:12]2)=[CH:7][CH:6]=1)C=C.C(N(CC)[C:20]1[CH:25]=CC=C[CH:21]=1)C>>[CH2:25]([C:14]1[C:5]([OH:4])=[CH:6][CH:7]=[C:8]2[C:13]=1[O:12][C:11](=[O:15])[CH:10]=[C:9]2[CH3:16])[CH:20]=[CH2:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7061N,N-DiethylanilineHCID 2389527-(Allyloxy)-4-methyl-2H-chromen-2-one

생성물 1

HCID 57131038-Allyl-7-hydroxy-4-methyl-chromen-2-one수율 65%

실험 절차

Crude 7-allyloxy-4-methylcoumarin (83.5 g, 0.381 mol) was dissolved in 250 ml of diethyl aniline with heating, and the solution was allowed to reflux for two hours. After the solution had cooled and some product had precipitated, petroleum ether (b.p. 30°-60° C., 760 ml) was added. A brown precipitate formed and was collected by filtration, washed with three small portions of petroleum ether, and dried in vacuo to obtain the crude product. Recrystallization from 600 ml of 95% EtOH gave the pure product (53.5 g, 74% recovery, 65% yield) of mp 192.5°-195.0° C. (lit. 193°-194° C.). TLC showed only a single spot.

후처리

  1. temperaturewith heating
  2. temperatureto reflux for two hours
  • temperatureAfter the solution had cooled
  • customsome product had precipitated
  • additionpetroleum ether (b.p. 30°-60° C., 760 ml) was added
  • customA brown precipitate formed
  • filtrationwas collected by filtration
  • washwashed with three small portions of petroleum ether
  • customdried in vacuo
  • 출처 및 근거

    ORD 기록
    ord-121167d53c244955836c4dd8d04576b3
    출처 데이터셋
    uspto-grants-1981_10
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04294847

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